Cubo Ana María, Soto Zandra Mileny, Cruz Miguel Ángel, Doyague María José, Sancho Verónica, Fraino Aurymar, Blanco Óscar, Puig Noemi, Alcoceba Miguel, González Marcos, Sayagués José María
Department of Obstetrics and Gynecology Department of Pathology Department of Radiology Department of Hematology University Hospital of Salamanca (IBSAL-HUS) CIBERONC, Salamanca, Spain.
Medicine (Baltimore). 2017 May;96(19):e6846. doi: 10.1097/MD.0000000000006846.
Primary lymphomas of the uterine cervix are a rare disease. They are often misdiagnosed because of their rarity and because they can be easily confused with a squamous cell carcinoma of the cervix, as they are usually presented as exophytic mass with vaginal bleeding as their most common symptoms. Nevertheless, considering that both the prognosis and the treatment are completely different between them, differential diagnosis should be taken into account.
A case of a 51-year-old woman with a primary diffuse large B-cell lymphoma of the cervix is presented.
Diagnosis of this tumor was a challenge for pathologists and clinicians, as four biopsies were needed to achieve a final diagnosis.
Patient was successfully treated with combined Rituximab and chemotherapy (R-CHOP) alone.
Complete remission, confirmed through biopsy, was reached after six courses of chemotherapy. At 2-years follow up, patient is alive and free of disease.
Considering that the prognosis and treatment of primary malignant lymphoma of the cervix are completely different than that of the squamous cell carcinoma, awareness of this disease should be considered in the differential diagnosis.
子宫颈原发性淋巴瘤是一种罕见疾病。由于其罕见性,且通常表现为外生性肿块,以阴道出血为最常见症状,容易与子宫颈鳞状细胞癌混淆,所以常被误诊。然而,鉴于两者的预后和治疗方法完全不同,应考虑进行鉴别诊断。
本文报道了一例51岁患有子宫颈原发性弥漫性大B细胞淋巴瘤的女性病例。
该肿瘤的诊断对病理学家和临床医生来说是一项挑战,需要进行四次活检才能得出最终诊断。
患者仅接受了利妥昔单抗联合化疗(R-CHOP),治疗成功。
六个疗程的化疗后,经活检确认达到完全缓解。在2年的随访中,患者存活且无疾病。
鉴于子宫颈原发性恶性淋巴瘤的预后和治疗与鳞状细胞癌完全不同,在鉴别诊断中应考虑对这种疾病的认识。